摘要
Complete oxidation of propane has attracted widespread attention in the treatment of volatile organic compounds (VOCs) from Fischer-Tropsch synthesis tail gas. Pt-based catalysts have been considered highly promising catalysts for the catalytic oxidation of propane due to their high-activity. However, despite the recognized importance of the synergistic effect between Pt nanoparticles (NPs) and support materials, the detailed reaction mechanism investigation remains limited. In this work, we demonstrate that the Pt/Al 2 O 3 catalyst exhibits improved propane catalytic performance, which is attributed to the synergistic interaction between Pt NPs and surface hydroxyl groups on the support. The improved Pt dispersion in Pt/Al 2 O 3 catalysts with smaller Pt NPs facilitates the spillover of gaseous oxygen species and the stabilization of active sites for propane oxidation. Furthermore, in- situ DRIFTS characterization and density functional theory (DFT) calculation confirm that surface hydroxyl groups on Al 2 O 3 effectively reduce the activation barrier for C-H bond cleavage, thereby improving the reactivity of propane molecules. This work provides a novel insight into metal-support synergy for propane oxidation, which offers strategic guidance for the rational design of efficient catalysts in hydrocarbon conversion processes.
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